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重组事件提示了亨廷顿舞蹈症基因的潜在位点。

Recombination events suggest potential sites for the Huntington's disease gene.

作者信息

MacDonald M E, Haines J L, Zimmer M, Cheng S V, Youngman S, Whaley W L, Wexler N, Bucan M, Allitto B A, Smith B

机构信息

Neurogenetics Laboratory, Massachusetts General Hospital, Boston 02114.

出版信息

Neuron. 1989 Aug;3(2):183-90. doi: 10.1016/0896-6273(89)90031-7.

Abstract

The Huntington's disease gene (HD) maps distal to the D4S10 marker in the terminal 4p16.3 subband of chromosome 4. Directed cloning has provided several DNA segments that have been grouped into three clusters on a physical map of approximately 5 X 10(6) bp in 4p16.3. We have typed RFLPs in both reference and HD pedigrees to produce a fine-structure genetic map that establishes the relative order of the clusters and further narrows the target area containing the HD gene. Despite the large number of meiotic events examined, the HD gene cannot be positioned relative to the most distal cluster. One recombination event with HD suggests that the terminal-most markers flank the disease gene; two others favor a telomeric location for the defect. Efforts to isolate the HD gene must be divided between these two distinct intervals until additional genetic data resolve the apparent contradiction in localization.

摘要

亨廷顿氏病基因(HD)定位于4号染色体4p16.3亚带末端的D4S10标记的远端。定向克隆已提供了几个DNA片段,这些片段在4p16.3约5×10⁶bp的物理图谱上被分成三个簇。我们在参考系和HD系谱中对限制性片段长度多态性(RFLP)进行了分型,以产生一个精细结构的遗传图谱,该图谱确定了簇的相对顺序,并进一步缩小了包含HD基因的目标区域。尽管检查了大量的减数分裂事件,但HD基因相对于最远端的簇仍无法定位。与HD的一次重组事件表明,最末端的标记位于疾病基因两侧;另外两次则支持该缺陷位于端粒位置。在获得更多遗传数据解决定位上明显的矛盾之前,分离HD基因的工作必须在这两个不同的区间进行。

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